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Idiopathic Acquired Transverse Myelitis

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This was a young adult who had weakness

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in the upper extremities.

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We have here the T1-weighted,

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T2-weighted, STIR, and post-gadolinium enhanced scans.

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On the T1-weighted scan,

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we have a low signal intensity lesion which

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shows bright signal intensity on the T2-weighted

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scan and the STIR images,

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and the cord appears to be expanded.

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On the post-gadolinium enhanced scan,

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we see that there is indeed contrast enhancement

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in somewhat of a peripheral nature.

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This is an example of a case where, frankly,

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I would not be able to distinguish between a

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neoplastic lesion, an inflammatory lesion,

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or a demyelinating lesion.

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All of them can cause cord expansion and usually

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show some element of contrast enhancement if

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it's an active demyelinating process

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within the demyelinating disorders.

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Because it is a long-segment

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disease that expands three segments,

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we would have to consider something.

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like neuromyelitis optica.

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Within the inflammatory infectious etiologies,

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there are any number of viral myelitis that can

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cause cord expansion and cord enhancement.

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The next step in this patient

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would be to do CSF sampling.

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The CSF sampling may be useful for CSF cytology,

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although for spinal cord lesions,

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it's not all that high yield.

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But you would include the demyelinating markers

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within the CSF, including myelin basic protein,

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among others. And you would do your culture

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and cells that may help you identify a bacterial

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or a viral myelitis.

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This particular case ended up being...

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I'm sorry, an idiopathic acquired

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transverse myelitis. That is,

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they never discovered any viral illnesses.

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the patient did not have any

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antecedent illnesses,

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the patient did not have an autoimmune disorder.

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And with steroids, this lesion resolved.

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Sometimes when you're looking at spinal

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cord lesions like this one,

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you're in multiple categories of disease,

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including neoplastic, demyelinating,

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and infectious inflammatory,

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and you just have to throw up your hands and say,

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'Recommend evaluation of the cerebrospinal fluid.'

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Besides throwing our hands up and recommending

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CSF sampling, what else could we do as radiologists?

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In this situation, it would be helpful to recommend

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evaluation of the brain and the remainder of the

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spinal cord evaluation. Why so? Well,

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if you saw multiple periventricular and

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subcortical lesions in the brain,

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you may go back to a demyelinating

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process that would suggest something like

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multiple sclerosis or neuromyelitis optica,

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or other demyelinating disorders.

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Similarly,

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if you found additional lesions in the spinal

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cord below the cervical region at

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the mid to lower thoracic spine,

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it might also suggest a demyelinating disorder,

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since that would be unusual for myelitis,

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which is usually a solitary lesion.

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You'd still have the category of neoplasm with

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multifocal astrocytomas or ependymomas

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if the patient had, for example,

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neurofibromatosis type 1 or

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neurofibromatosis type 2.

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So in addition to recommending CSF sampling,

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recommend evaluation of the brain for other

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demyelinating lesions or the remainder

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of the spinal cord.

Report

Description

Faculty

David M Yousem, MD, MBA

Professor of Radiology, Vice Chairman and Associate Dean

Johns Hopkins University

Tags

Spine

Non-infectious Inflammatory

Neuroradiology

Neoplastic

Musculoskeletal (MSK)

MRI

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